Effects of opioid blockade with naltrexone and distraction on cold and ischemic pain in hypertension

J Behav Med. 2007 Feb;30(1):59-68. doi: 10.1007/s10865-006-9084-1. Epub 2007 Jan 5.

Abstract

Essential hypertension is characterised by reduced pain sensitivity. Hypertensive hypoalgesia has been attributed to elevated endogenous opioids and/or increased activation of descending pain modulation systems. A double-blind placebo-controlled design compared the effects of naltrexone and placebo on cold and ischemic pain in unmedicated newly-diagnosed patients with essential hypertension. Patients performed a cold pressor task while resting and while performing a distracting secondary task. They also performed a forearm ischemia task while resting. Although the cold pressor and ischemia tasks elicited significant increases in pain and blood pressure, pain ratings and pressor responses did not differ between naltrexone and placebo. Cold pain was reduced by distraction compared to rest. The finding that opioid blockade with naltrexone did not moderate the pain and pressor responses to cold and ischemia suggests that pain and associated blood pressure responses are not modulated by opioids in hypertension. The finding that the distracting secondary task successfully reduced pain ratings suggests normal supraspinal pain modulation in essential hypertension.

Publication types

  • Clinical Trial
  • Research Support, N.I.H., Extramural

MeSH terms

  • Adult
  • Attention*
  • Cold Temperature*
  • Double-Blind Method
  • Female
  • Heart Rate / physiology
  • Humans
  • Hypertension / epidemiology*
  • Hypertension / metabolism*
  • Male
  • Myocardial Ischemia / epidemiology*
  • Myocardial Ischemia / metabolism*
  • Naltrexone / administration & dosage
  • Naltrexone / pharmacology*
  • Narcotic Antagonists / administration & dosage
  • Narcotic Antagonists / pharmacology*
  • Pain / diagnosis
  • Pain / epidemiology*
  • Pain / metabolism*
  • Pain Measurement
  • Touch
  • beta-Endorphin / antagonists & inhibitors*
  • beta-Endorphin / metabolism*

Substances

  • Narcotic Antagonists
  • Naltrexone
  • beta-Endorphin